Implement Germline Variant Exploration tool that will enable users to navigate across millions of annotated germline variants from INCLUDE participants with known co-occurring conditions

[ByroneCole-SageBionetworks]

• We will first leverage the variant data for the studies that are also part of the KF Program. ( KF code: KF-CHDALL, KF-CHD. INCLUDE code: HTP, DS-PCGC, DS-360CHD, DS-COG-ALL)

• The somatic mutations will be implemented in a later phase